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  1. Arl3 Rod-Specific Knockout Displays RP-Like Photoreceptor Degeneration

    This abstract was presented today at the 2014 Association for Research in Vision and Opthalmology (ARVO) meetings in Orlando, Florida by Christin Hanke, Houbin Zhang, Cecilia D. Gerstner, Jeanne M. Frederick AND Wolfgang Baehr. Full size poster can be downloaded here. Purpose: Arf-like protein 3 (Arl3) localizes predominantly in the photoreceptor inner segment. Germline Arl3 knockout mice do not […]

    May 4, 2014 — Read more No Comments
  2. Notable Paper: Long-term RNA interference gene therapy in a dominant retinitis pigmentosa mouse model

    Hereditary retinal dystrophies (retinitis pigmentosa, Leber congenital amaurosis, cone-rod dystrophies, macular degeneration) are characterized by loss of visual function, sometimes starting during early childhood, other times in late adulthood.  About 30% of these dystrophies are inherited in an autosomal dominant fashion (RetNet), caused by gain-of-function mutant alleles which encode a malignant form of a normal […]

    Nov 2, 2011 — Read more No Comments